Structural highlights
Disease
[ECHA_HUMAN] Mitochondrial trifunctional protein deficiency;Acute fatty liver of pregnancy;Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. [ECHB_HUMAN] Mitochondrial trifunctional protein deficiency. The disease is caused by mutations affecting the gene represented in this entry.
Function
[ECHA_HUMAN] Bifunctional subunit.